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Philips North America Llc

Philips North America Llc Recalls

All product recalls associated with Philips North America Llc.

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Recall Summary

Total Recalls

1000

Past Year

631

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 381–400 of 10391 recalls

Evolution Upgrade 1.5T (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

Kendall SCD Comfort Sleeve (Cardinal Health) – Software Pressure Error (2025)

Incorrect software logic may cause frequent E1 errors (system high pressure). Issue may cause delay in treatment or therapy.

Moderate

FDAMay 13, 2025AK, CA, FL +2 more• Cardinal Health 200, LLC

SmartPath 1.5T (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025

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Nationwide

• Philips North America Llc

SmartPath Ingenia Elition X (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

Ingenia 3.0T CX (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

Ingenia Ambition S (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

SCD Comfort Sleeve (Cardinal Health) – Software Pressure Error (2025)

Incorrect software logic may cause frequent E1 errors (system high pressure). Issue may cause delay in treatment or therapy.

Moderate

FDAMay 13, 2025AK, CA, FL +2 more• Cardinal Health 200, LLC

Roasted Salted Cashews (Honey Heaven) – Undeclared Hazelnut (2025)

Undeclared Allergen

Undeclared hazelnut. The Oregon Trail Mix contains visible hazelnut and was mis-labeled as Organic Roasted Salted Cashews, but the label does not declare hazelnut.

Class IIModerate

FDAMay 13, 2025CA, IN, OR +1 more• Honey Heaven Wholesale Inc

MR 7700 Upgrade (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

Ingenia Elition S (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

HemoCue Glucose Microcuvettes (HemoCue) – Stability Concern (2025)

Glucose microcuvettes experienced transit time outside of limits, so stability through the whole microcuvette lifetime can no longer be guaranteed. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency, and purity of the product. This failure could increase the probability of an incorrect test result or a delayed test result.

Moderate

FDAMay 12, 2025Nationwide• HemoCue AB Kuvettgatan 1 Angelholm Sweden

Baxter Novum IQ Syringe Pump (Baxter) – Syringe Detection Issue (2025)

Baxter has identified a design issue which may cause the pump to detect the presence of a syringe flange when no syringe is loaded. When this issue occurs, the pumps 'user interface becomes stuck on the "Remove Syringe" screen when an infusion is complete, and the syringe is unloaded. A System Error 21502 (Flange Sensor Failure) may occur. Please note this issue only affects a subset of Novum IQ syringe pumps manufactured or repaired after July 4, 2023.

Moderate

FDAMay 12, 2025Nationwide• Baxter Healthcare Corporation

Welch Allyn Battery (Baxter) – Short Circuit Risk (2025)

Fire/Burn Risk

The replacement rechargeable batteries inserted into the Welch Allyn PocketScope handles have the potential to cause a short circuit in the handle, which can lead to exposure to excessive heat and user burns.

High

FDAMay 9, 2025Nationwide• Baxter Healthcare Corporation

2026 Thor Motor Coach Outlaw (Thor) – Step/Ladder Problem (2025)

Thor Motor Coach (TMC) is recalling certain 2025-2026 TMC Outlaw motorhomes, equipped with a removable step assembly. The clip-on bracket mounting bolts may come loose, allowing the steps to detach.

High

NHTSAMay 8, 2025Nationwide• THOR MOTOR COACH

Sabudana Khichadi (Shastha Foods) – Undeclared Allergens (2025)

Undeclared Allergen

Undeclared allergens (milk and/or peanuts).

Class IIModerate

FDAMay 8, 2025CA, UT, WA• Bondsforever, Inc dba Shastha Foods

Pohe (Shastha Foods) – Undeclared Allergens (2025)

Undeclared Allergen

Undeclared allergens (milk and/or peanuts).

Class IIModerate

FDAMay 8, 2025CA, UT, WA• Bondsforever, Inc dba Shastha Foods

Jumbo Pumpkin Seeds (Organic Traditions) – Salmonella Risk (2025)

Salmonella

Product may be contaminated with Salmonella

Class IHigh

FDAMay 7, 2025NJ, NY, VA• Advantage Health Matters Inc.

Affinity 4 Birthing Bed (Baxter) – Signal Wire Crimp (2025)

There is a potential for improper crimps on the signal wires of the actuators which could result in a loss of ability to lower the bed or the foot section of the bed.

High

FDAMay 6, 2025Nationwide• Baxter Healthcare Corporation

Frozen Shrimp (Chicken of the Sea) – Undeclared Sulfites (2025)

Undeclared Allergen

Frozen Raw Peeled & Deveined tail on, shrimp contains undeclared sulfites

Class IHigh

FDAMay 6, 2025CO, IN• TRI-UNION FROZEN PRODUCTS INC DBA CHICKEN OF THE SEA FROZEN FOOD

Endurance Boost Capsules (EnShiShiXiangNi) – Undeclared Sildenafil (2025)

Marketed without approved NDA/ANDA: The product has been found to be tainted with Sildenafil and Propoxyphenylsildenafil (a sildenafil analogue).

Class IHigh

FDAMay 6, 2025Nationwide• EnShiShiXiangNiShangMaoYouXianGongSi